Systems and methods for biosensing and microresonator sensors for same

Abstract

A biosensor system is provided for detecting biological species such as bacteria, proteins, viruses, spores and DNA or RNA. The biosensor system may also be able to distinguish between Gram positive and Gram negative bacteria. In some embodiments, the analyte solution flows past a detector surface to a filter, which traps the analyte. The analyte is then washed back past the detector surface, thus increasing the number of analyte species that become attached to the surface. The detector may include an optical microresonator that is optically coupled via waveguides to a light source and an optical detector. One of the waveguides may be provided with a wavelength selective reflector to increase the amount of probe light coupled into the microresonator or to increase the fraction of the signal light detected by the optical detector.

Description

FIELD OF THE INVENTION [0001] The invention is directed generally to systems and methods for detecting bacteria, including optical sensors that use microresonators. BACKGROUND [0002] The detection of biological species is an important analytical technique in several industries, including the food industry, environmental monitoring, and health care, e.g. for the prevention of post-surgical infection. For example, traditional methods of detecting bacteria require the culturing of microorganisms. While these methods provide a desired level of sensitivity, they require highly trained laboratory personnel and typically need days to obtain results. [0003] Post-surgery infections constitute the most common infection for surgical patients. In many cases, bacteria still remain on the skin after the skin has been prepared for surgery. About 20% of the population have high bacteria counts on the skin, i.e. more than 1000 CFU cm−2 and represent those who are at greatest risk of infection. Accor...

AI Technical Summary

Benefits of technology

[0004] There remains a need, therefore, for a method of detecting biological species, such as bacteria (both Gram positive and Gram negative), viruses, spores, proteins and DNA and RNA strands, that is sensitive, less expensive than conventional methods and produces results rapidly.

Problems solved by technology

While these methods provide a desired level of sensitivity, they require highly trained laboratory personnel and typically need days to obtain results.

LAL cannot, however, distinguish between bacteria-surface bound LPS and free (soluble) LPS in solution.

The separation of soluble LPS from intact bacteria is a very challenging issue.

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